Primary Device ID | 04260277173579 |
NIH Device Record Key | 71dfbc6e-954d-4f70-8663-fce23e99711f |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Manual TruCut Biopsy Cannula |
Version Model Number | MBY-1050-16-0075 |
Company DUNS | 320405061 |
Company Name | Möller Medical GmbH |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | false |
MRI Safety Status | Labeling does not contain MRI Safety Information |
Human Cell/Tissue Product | false |
Device Kit | false |
Device Combination Product | false |
Single Use | true |
Lot Batch | true |
Serial Number | false |
Manufacturing Date | true |
Expiration Date | true |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | true |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 04260277173418 [Primary] |
GS1 | 04260277173579 [Package] Contains: 04260277173418 Package: [10 Units] In Commercial Distribution |
KNW | Instrument, Biopsy |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2018-09-17 |
Device Publish Date | 2018-08-17 |
04260277173647 | MBY-1050-14-0200 |
04260277173630 | MBY-1050-14-0152 |
04260277173623 | MBY-1050-14-0114 |
04260277173616 | MBY-1050-14-0075 |
04260277173609 | MBY-1050-16-0200 |
04260277173593 | MBY-1050-16-0152 |
04260277173586 | MBY-1050-16-0114 |
04260277173579 | MBY-1050-16-0075 |
04260277173562 | MBY-1050-17-0200 |
04260277173555 | MBY-1050-17-0152 |
04260277173548 | MBY-1050-17-0114 |
04260277173531 | MBY-1050-17-0075 |
04260277173524 | MBY-1050-18-0200 |
04260277173517 | MBY-1050-18-0152 |
04260277173500 | MBY-1050-18-0114 |
04260277173494 | MBY-1050-18-0075 |